List of variants in gene combination KCNE2, LOC105372791 reported as benign for atrial fibrillation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_172201.2(KCNE2):c.-79G>A	rs41260744	0.07525
NM_172201.2(KCNE2):c.25C>G (p.Gln9Glu)	rs16991652	0.00468

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